Dr Rebecca Mitchell
Dr Rebecca Mitchell
Dr Beck Mitchell is an experienced developmental paediatrician with expertise in complex developmental disability. Dr Mitchell is a senior research fellow with the Neurodevelopment Flagship and works as a clinical developmental paediatrician.
Dr Mitchell's PhD investigated the developmental phenotype in children with a genetic condition called tuberous sclerosis complex (TSC). Dr Mitchell's research focussed particularly on the presentation of autism and intellectual disability, and the associations between 'disease factors', such as genetic changes, epilepsy and structural brain changes and how these are linked with developmental outcomes. Dr Mitchell also has an interest in the synthesis of evidence, and has undertaken several systematic reviews with meta-analysis.
Currently, Dr Mitchell is co-lead on the Neurodevelopment Flagship SIGNAL study. This study is investigating changes over time in the developmental profile of children with genetic conditions, including TSC and neurofibromatosis type 1, and understanding the factors that impact on development.
Dr Mitchell's PhD investigated the developmental phenotype in children with a genetic condition called tuberous sclerosis complex (TSC). Dr Mitchell's research focussed particularly on the presentation of autism and intellectual disability, and the associations between 'disease factors', such as genetic changes, epilepsy and structural brain changes and how these are linked with developmental outcomes. Dr Mitchell also has an interest in the synthesis of evidence, and has undertaken several systematic reviews with meta-analysis.
Currently, Dr Mitchell is co-lead on the Neurodevelopment Flagship SIGNAL study. This study is investigating changes over time in the developmental profile of children with genetic conditions, including TSC and neurofibromatosis type 1, and understanding the factors that impact on development.
Dr Beck Mitchell is an experienced developmental paediatrician with expertise in complex developmental disability. Dr Mitchell is a senior research fellow with the Neurodevelopment Flagship and works as a clinical developmental paediatrician.
Dr...
Dr...
Dr Beck Mitchell is an experienced developmental paediatrician with expertise in complex developmental disability. Dr Mitchell is a senior research fellow with the Neurodevelopment Flagship and works as a clinical developmental paediatrician.
Dr Mitchell's PhD investigated the developmental phenotype in children with a genetic condition called tuberous sclerosis complex (TSC). Dr Mitchell's research focussed particularly on the presentation of autism and intellectual disability, and the associations between 'disease factors', such as genetic changes, epilepsy and structural brain changes and how these are linked with developmental outcomes. Dr Mitchell also has an interest in the synthesis of evidence, and has undertaken several systematic reviews with meta-analysis.
Currently, Dr Mitchell is co-lead on the Neurodevelopment Flagship SIGNAL study. This study is investigating changes over time in the developmental profile of children with genetic conditions, including TSC and neurofibromatosis type 1, and understanding the factors that impact on development.
Dr Mitchell's PhD investigated the developmental phenotype in children with a genetic condition called tuberous sclerosis complex (TSC). Dr Mitchell's research focussed particularly on the presentation of autism and intellectual disability, and the associations between 'disease factors', such as genetic changes, epilepsy and structural brain changes and how these are linked with developmental outcomes. Dr Mitchell also has an interest in the synthesis of evidence, and has undertaken several systematic reviews with meta-analysis.
Currently, Dr Mitchell is co-lead on the Neurodevelopment Flagship SIGNAL study. This study is investigating changes over time in the developmental profile of children with genetic conditions, including TSC and neurofibromatosis type 1, and understanding the factors that impact on development.
Top Publications
- Mitchell, RA, Lami, F, Barton, SM, Harvey, AS, Williams, K. Deep developmental phenotyping in children with tuberous sclerosis complex, with and without autism.. Dev Med Child Neurol 67(9) : 1165 -1175 2025 view publication
- Payne, JM, Haebich, KM, Mitchell, R, Bozaoglu, K, Giliberto, E, Lockhart, PJ, Maier, A, Velasco, S, Ball, G, North, KN, et al. Brain volumes in genetic syndromes associated with mTOR dysregulation: a systematic review and meta-analysis.. Mol Psychiatry 30(4) : 1676 -1688 2025 view publication
- Mitchell, RA, Mitchell, M, Williams, K. The autism spectrum disorder phenotype in children with tuberous sclerosis complex: A systematic review and meta-analysis.. Dev Med Child Neurol 64(10) : 1214 -1229 2022 view publication
- Mitchell, RA, Barton, SM, Harvey, AS, Ure, AM, Williams, K. Factors associated with autism spectrum disorder in children with tuberous sclerosis complex: a systematic review and meta-analysis.. Dev Med Child Neurol 63(7) : 791 -801 2021 view publication
- Mitchell, R, Barton, S, Harvey, AS, Williams, K. Risk factors for the development of autism spectrum disorder in children with tuberous sclerosis complex: protocol for a systematic review.. Syst Rev 6(1) : 49 2017 view publication
Page 1 of 2
Career information
Share //
